Curing and Alignment of Liquid Crystalline Epoxy Networks

1990 ◽  
Vol 203 ◽  
Author(s):  
C. K. Ober ◽  
G. G. Barclay ◽  
K I. Papathomas ◽  
D. W. Wang

ABSTRACTLiquid crystalline epoxy networks have been prepared from glycidyl terminated polyether oligomers of varying molecular weight. These oligomers were prepared by functionalizing hydroxy terminated oligomers based on 4,4'- dihydroxy-α-methylstilbene and α,ω-dibromoalkanes with glycidyl groups. Curing of these oligomers was carried out either within their nematic mesophase or in their isotropic state. Different thermal properties were observed after curing under these two sets of conditions. Extremely low values of the coefficient of thermal expansion in the range of 15 to 60 ppm/°C were achieved. To produce aligned thermosets, orientation of the liquid crystalline phase was induced during the curing process by a magnetic field. Orientation of these networks was measured by wide angle x-ray diffraction (WAXD).

1999 ◽  
Vol 559 ◽  
Author(s):  
Derek M. Lincoln ◽  
Elliot P. Douglas

ABSTRACTWe have investigated the effect of various processing variables on the magnetic field orientation of a liquid crystalline epoxy. By using a modified fractional factorial design, we created an empirical model which can be used to predict the degree of orientation as a function of these variables. The model predicts the correct qualitative trends, namely that orientation increases with increasing magnetic field strength, increases with increasing time in the field, and decreases with increasing B-staging. The model also reveals some surprising effects of B-staging on the degree of orientation.


1991 ◽  
Vol 227 ◽  
Author(s):  
C. K Ober ◽  
G. G. Barclay

ABSTRACTNew liquid crystalline thermosets have been prepared from end-functional monomers and oligomers of varying molecular weight. Both triazine and epoxy networks were explored. Of primary interest was the exploitation of the mesophase properties of these networks for developing polymers with high thermal stability and low coefficients of thermal expansion (CTE). Curing was carried out either within the nematic mesophase or the isotropic phase of the prepolymers. Transition temperatures associated with the mesophase were observed to change after curing under these two sets of conditions. The networks with the highest crosslink density were found to exhibit the lowest CTE values. Crosslinking of these thermosets was also carried out in the presence of a 13.5 Tesla magnetic field to determine the effect of orienting fields on the curing of the LC network. Orientation parameters as measured by wide angle x-ray diffraction were as high as 0.6. Values of the coefficient of thermal expansion as low as 15 ppm were achieved in the aligned direction. Of the two resin types, those with the triazine crosslinks had the lowest thermal expansion coefficient. Other thermal properties of these networks will be discussed.


1991 ◽  
Vol 227 ◽  
Author(s):  
Joonhyun Nam ◽  
Tomohiro Fukai ◽  
Thein Kyu

ABSTRACTA thermotropic liquid crystalline copolymer consisting of bisphenol E diacetate, isophthalic acid and 2,6-naphthalene dicarboxylic acid was blended with polyether imide by dissolving in a mixed solvent of phenol/1,1,2,2-tetrachloroethane in a ratio of 60/40 w/w and co-precipitating the ternary solution in non-solvent (methanol). Wide-angle x-ray diffraction and differential scanning calorimetry studies revealed that the blends were completely amorphous with a single glass transition temperature. The single phase was probably entrapped during solvent removal, but these mixes were unstable and phase separated upon heating. Mesophase structure developed in the LCP rich region with continued annealing. The evolution of crystalline texture was monitored by time-resolved wide-angle x-ray diffraction following a temperature jump from ambient to 265 °C. The recrystallization process of LCP was found to slow down in the blend state relative to that of the neat LCP.


1998 ◽  
Vol 31 (15) ◽  
pp. 4730-4738 ◽  
Author(s):  
Brian C. Benicewicz ◽  
Mark E. Smith ◽  
Jim D. Earls ◽  
Ralph D. Priester ◽  
Stefan M. Setz ◽  
...  

2010 ◽  
Vol 428-429 ◽  
pp. 144-149
Author(s):  
Xiao Dong Chen ◽  
Nan Qiao Zhou ◽  
Hai Zhang

A thermotropic liquid crystalline polyurethane (LCPU) was synthesized by the polyaddition reaction of 3,3'-dimethyl-4,4'-biphenylene diisocyanate (TODI) with 4,4-bis(6-hydroxyhexoxy)biphenyl (BHHBP). The liquid crystalline behavior of the polymer was investigated by differential scanning calorimetry (DSC), polarized optical microscopy (POM), wide angle X-ray diffraction (WAXD). The LCPU exhibited a nematic phase with a threaded texture and had a wide mesophase temperature range. And thermogravimetric analysis (TGA) indicated the decomposition temperature of the LCPU was >300°C. The observation of POM showed that the LCPU was a thermotropic nematic liquid crystalline polymer at certain temperature range.


2003 ◽  
Vol 36 (4) ◽  
pp. 986-990 ◽  
Author(s):  
Jaroslaw Janicki

Novel melt-processable molecular composites were obtained from isotactic polypropylene (iPP) and liquid-crystalline oligoester (LCO). The nanostructure and thermal behaviour of molecular composites were examined by real-time synchrotron small-angle X-ray scattering and wide-angle X-ray diffraction methods, and differential scanning calorimetry. The synthesized oligoester, with low melting temperature (391 K), exhibits the ability to form a thermotropic mesophase. It was shown that strong rigid rod-like macromolecules of LCO are dispersed at the molecular scale in iPP matrix and act as reinforcing fibres.


2007 ◽  
Vol 168 (1) ◽  
pp. 37-41 ◽  
Author(s):  
Valerio Causin ◽  
Carla Marega ◽  
Pietro Carresi ◽  
Sergio Schiavone ◽  
Antonio Marigo

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